Canonical Allele Identifier: CA10643218

Gene: SPART

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.36302214_36302218del , CM000675.2:g.36302214_36302218del	GRCh38
NC_000013.10:g.36876351_36876355del , CM000675.1:g.36876351_36876355del	GRCh37
NC_000013.9:g.35774351_35774355del	NCBI36
NG_011559.1:g.72966_72970del
NG_011559.2:g.72966_72970del

Transcript Alleles

HGVS	Amino-acid Change
NM_015087.5:c.*2150_*2154del MANE Select	NP_055902.1:n.*2150_*2154del
ENST00000438666.7:c.*2150_*2154del MANE Select	ENSP00000406061.2:n.*2150_*2154del
NM_001142294.1:c.*2150_*2154del	NP_001135766.1:n.*2150_*2154del
NM_001142294.2:c.*2150_*2154del	NP_001135766.1:n.*2150_*2154del
NM_001142295.1:c.*2150_*2154del	NP_001135767.1:n.*2150_*2154del
NM_001142295.2:c.*2150_*2154del	NP_001135767.1:n.*2150_*2154del
NM_001142296.1:c.*2150_*2154del	NP_001135768.1:n.*2150_*2154del
NM_001142296.2:c.*2150_*2154del	NP_001135768.1:n.*2150_*2154del
NM_015087.4:c.*2150_*2154del	NP_055902.1:n.*2150_*2154del
ENST00000355182.8:c.*2150_*2154del	ENSP00000347314.4:n.*2150_*2154del
ENST00000438666.6:c.*2150_*2154del	ENSP00000406061.2:n.*2150_*2154del
ENST00000451493.5:c.*2150_*2154del	ENSP00000414147.1:n.*2150_*2154del
ENST00000650221.1:c.*2150_*2154del	ENSP00000497209.1:n.*2150_*2154del
XM_005266313.5:c.*2150_*2154del	XP_005266370.1:n.*2150_*2154del
XM_005266314.3:c.*2150_*2154del	XP_005266371.1:n.*2150_*2154del
XM_005266315.3:c.*2150_*2154del	XP_005266372.1:n.*2150_*2154del
XM_005266317.3:c.*2150_*2154del	XP_005266374.1:n.*2150_*2154del
XM_011535012.2:c.*2150_*2154del	XP_011533314.1:n.*2150_*2154del
XM_024449334.1:c.*2150_*2154del	XP_024305102.1:n.*2150_*2154del
XR_001749523.2:n.4494_4498del